CYTOKINE-BINDING PROTEINS IN THE LUNG

被引:40
作者
BONNER, JC [1 ]
BRODY, AR [1 ]
机构
[1] TULANE UNIV, MED CTR, DEPT PATHOL, LUNG BIOL PROGRAM, NEW ORLEANS, LA 70112 USA
关键词
GROWTH-PROMOTING CYTOKINES; TISSUE REPAIR; INFLAMMATORY LUNG DISEASE;
D O I
10.1152/ajplung.1995.268.6.L869
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Numerous cytokines and growth factors signal the normal processes of tissue maintenance and remodeling in the lung, yet the aberrant expression of these peptide mediators is involved in a variety of pulmonary diseases. Furthermore, several different binding proteins function in controlling the extracellular levels of many of these cytokines in the lung. For example, a variety of cytokines and growth factors bind to and are regulated by the ubiquitous proteinase inhibitor, (alpha(2))-macroglobulin. The insulin-like growth factors are controlled by a specific class of six different insulin-like growth factor binding proteins. The transforming growth factor-beta family and fibroblast growth factors interact with extracellular matrix proteins. Several growth factor receptors are shed into the extracellular milieu where they retain a functional binding domain and thereby act as specific binding proteins. Cytokine-binding proteins appear to have a diversity of functions and may serve as extracellular cytokine reservoirs, protective shields against proteolytic degradation of cytokines, modifiers of cytokine-induced biological activity, or as clearance avenues for cytokines. The wide spectrum of cytokine-regulating molecules is important in cell-cell communications under normal conditions, whereas cytokine-binding protein dysfunction could contribute to a number of pulmonary diseases.
引用
收藏
页码:L869 / L878
页数:10
相关论文
共 109 条
[1]   MEMBRANE-ANCHORED AND SOLUBLE FORMS OF BETAGLYCAN, A POLYMORPHIC PROTEOGLYCAN THAT BINDS TRANSFORMING GROWTH FACTOR-BETA [J].
ANDRES, JL ;
STANLEY, K ;
CHEIFETZ, S ;
MASSAGUE, J .
JOURNAL OF CELL BIOLOGY, 1989, 109 (06) :3137-3145
[2]   RECEPTOR-BINDING AND HEPARIN-BINDING DOMAINS OF BASIC FIBROBLAST GROWTH-FACTOR [J].
BAIRD, A ;
SCHUBERT, D ;
LING, N ;
GUILLEMIN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (07) :2324-2328
[3]   PRODUCTION OF IGF-BINDING PROTEINS BY VASCULAR ENDOTHELIAL-CELLS [J].
BAR, RS ;
HARRISON, LC ;
BAXTER, RC ;
BOES, M ;
DAKE, BL ;
BOOTH, B ;
COX, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (02) :734-739
[4]  
BARRETT AJ, 1981, METHOD ENZYMOL, V80, P737
[5]   INTERACTION OF ALPHA2-MACROGLOBULIN WITH PROTEINASES - CHARACTERISTICS AND SPECIFICITY OF REACTION, AND A HYPOTHESIS CONCERNING ITS MOLECULAR MECHANISM [J].
BARRETT, AJ ;
STARKEY, PM .
BIOCHEMICAL JOURNAL, 1973, 133 (04) :709-&
[6]   BASIC FIBROBLAST GROWTH-FACTOR BINDS TO SUBENDOTHELIAL EXTRACELLULAR-MATRIX AND IS RELEASED BY HEPARITINASE AND HEPARIN-LIKE MOLECULES [J].
BASHKIN, P ;
DOCTROW, S ;
KLAGSBRUN, M ;
SVAHN, CM ;
FOLKMAN, J ;
VLODAVSKY, I .
BIOCHEMISTRY, 1989, 28 (04) :1737-1743
[7]  
BERTINI R, 1993, EUR CYTOKINE NETW, V4, P39
[8]  
BLUM WF, 1989, ENDOCRINOLOGY, V25, P766
[9]  
BONNER JC, 1992, J BIOL CHEM, V267, P12837
[10]   INHIBITION OF PLATELET-DERIVED GROWTH FACTOR-BB-INDUCED FIBROBLAST PROLIFERATION BY PLASMIN-ACTIVATED ALPHA(2)-MACROGLOBULIN IS MEDIATED VIA AN ALPHA(2)-MACROGLOBULIN RECEPTOR LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN-DEPENDENT MECHANISM [J].
BONNER, JC ;
BADGETT, A ;
HOFFMAN, M ;
LINDROOS, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :6389-6395